Para-chord Liquid
NDC Package 64578-0073-1
Package Information
Para-chord (homeopathic liquid) liquids is a human otc drug administered via oral route. This formulation utilizes a liquid delivery system. Marketed by Energetix Corporation, this product is identified by NDC 64578-0073.
Identification & Billing
Clinical Specifications
- ARTEMISIA ABROTANUM FLOWERING TOP 12 [hp_X]/59.1mL
- ARTEMISIA CINA PRE-FLOWERING TOP 5 [hp_X]/59.1mL
- ARTEMISIA VULGARIS ROOT 12 [hp_X]/59.1mL
- DRYOPTERIS FILIX-MAS ROOT 4 [hp_X]/59.1mL
- DYSPHANIA AMBROSIOIDES 12 [hp_X]/59.1mL
- GRAPHITE 12 [hp_X]/59.1mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 15 [hp_X]/59.1mL
- PEUMUS BOLDUS LEAF 4 [hp_X]/59.1mL
- PUNICA GRANATUM ROOT BARK 12 [hp_X]/59.1mL
- SILICON DIOXIDE 12 [hp_X]/59.1mL
- SODIUM PHOSPHATE, DIBASIC 12 [hp_X]/59.1mL
- SPIGELIA ANTHELMIA 6 [hp_C]/59.1mL
- TANACETUM VULGARE TOP 12 [hp_X]/59.1mL
- TEUCRIUM MARUM 5 [hp_X]/59.1mL
- WHITE MUSTARD SEED 12 [hp_X]/59.1mL
Regulatory & Marketing
Hierarchy Structure
- 64578 - Energetix Corporation
- 64578-0073 - Para-chord
- 64578-0073-1 - 59.1 mL in 1 BOTTLE, DROPPER
- 64578-0073 - Para-chord
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 64578-0073-1 identifies a specific commercial package of 59.1 ml in 1 bottle, dropper of Para-chord, a human over the counter drug labeled by Energetix Corporation. This liquid is formulated for oral use and contains artemisia abrotanum flowering top; artemisia cina pre-flowering top; artemisia vulgaris root; dryopteris filix-mas root; dysphania ambrosioides; graphite; oyster shell calcium carbonate, crude; peumus boldus leaf; punica granatum root bark; silicon dioxide; sodium phosphate, dibasic; spigelia anthelmia; tanacetum vulgare top; teucrium marum; white mustard seed as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Energetix Corporation on July 07, 2015. The current certification is valid through December 31, 2026.
How is this Energetix Corporation product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 64578007301. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.